chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
15304117304118G18GENICheterozygous140915424
15528838528839G16GENICheterozygous403368959
15528838528839GC16GENICheterozygous403368960
15719829719830G23GENICheterozygous403368983
15719829719830GA23GENICheterozygous403368984
15752007752008AG31GENICheterozygous154931878
15752007752008A31GENICheterozygous403656536
15834381834382A12GENICpossibly homozygous403368999
15834381834382AT12GENICheterozygous403369000
15856688856689G19GENICheterozygous403369001
15856688856689GA19GENICheterozygous403369002
15955721955722TA17GENICheterozygous154936673
15955721955722T17GENICheterozygous403369010
15922988922989T36GENICheterozygous141120974
15589543589544GT29GENICpossibly homozygous139652049
15955325955326G30GENICheterozygous403743172
15955325955326GC30GENICheterozygous403743173